P3.42 Mutation in the ryanodine receptor (RYR1) gene in a family with slowly progressive axial muscular dystrophy

Saved in:
Bibliographic Details
Published inNeuromuscular disorders : NMD Vol. 21; no. 9; pp. 694 - 695
Main Authors Torbergsen, T, Karime, B, Løseth, S
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.10.2011
Subjects
Neurology
Online AccessGet full text

Cover

More Information
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0960-8966
1873-2364
DOI:10.1016/j.nmd.2011.06.936